Canonical Allele Identifier: CA111096857
Gene: LINC02268 HGNC NCBI

Linked Data

dbSNP Id: rs973092492
gnomAD v2: 4-175027449-T-G
gnomAD v3: 4-174106298-T-G
gnomAD v4: 4-174106298-T-G
MyVariant Identifiers: chr4:g.175027449T>G (hg19) chr4:g.174106298T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.174106298T>G , CM000666.2:g.174106298T>G GRCh38
NC_000004.11:g.175027449T>G , CM000666.1:g.175027449T>G GRCh37
NC_000004.10:g.175264024T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125896.1:n.276-8469A>C
XR_939484.1:n.877+18659T>G
XR_939485.1:n.877+18659T>G
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